A Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate DMF (Drug Master File) is a document detailing the whole manufacturing process of Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate active pharmaceutical ingredient (API) in detail. Different forms of Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate DMFs exist exist since differing nations have different regulations, such as Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate DMF submitted to regulatory agencies in the US is known as a USDMF. Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate USDMF includes data on Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ammonium, (m-hydroxyphenyl)trimethyl-, methyl sulfate, dimethylcarbamate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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